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急性心肌梗死早期静脉注射阿尼普酶对梗死面积及左心室功能的影响。APSIM研究组

Effects on infarct size and left ventricular function of early intravenous injection of anistreplase in acute myocardial infarction. The APSIM Study Investigators.

作者信息

Bassand J P, Bernard Y, Lusson J R, Machecourt J, Cassagnes J, Borel E

机构信息

Service de Cardiologie, Hôpital Universitaire Saint Jacques, Besançon, France.

出版信息

Clin Cardiol. 1990 Mar;Suppl 5:V39-44; discussion V67-72. doi: 10.1002/clc.4960131310.

Abstract

A total of 231 patients suffering from a first acute myocardial infarction were randomly allocated within 4 hours following the onset of symptoms either to anistreplase or anisoylated plasminogen streptokinase activator complex (APSAC), 30 U over 5 minutes, or to conventional heparin therapy, 5000 IU in bolus injection. Heparin was reintroduced in both groups 4 h after initial therapy at a dosage of 500 IU/kg per day. A total of 112 patients received anistreplase and 119 received heparin within a mean period of 188 +/- 62 min following the onset of symptoms. Infarct size was estimated from single photon emission computerized tomography and expressed in percentage of the total myocardial volume. The patency rate of the infarct-related artery was 77% in the anistreplase group and 36% in the heparin group (p less than 0.001). Left ventricular ejection fraction determined from contrast angiography was significantly higher in the anistreplase group than in the heparin group (6 absolute percentage point difference). A significant 31% reduction in infarct size was found in the anistreplase group (33% for the anterior wall infarction subgroup [p less than 0.05] and 16% for the inferior wall infarction subgroup, NS). A close inverse relation was found between the values of left ventricular ejection fraction and infarct size (r = -.73, p less than 0.01). In conclusion, early infusion of anistreplase in acute myocardial infarction produced a high early patency rate, a significant limitation of infarct size, and a significant preservation of left ventricular systolic function, mainly in the anterior wall infarctions.

摘要

共有231例首次发生急性心肌梗死的患者在症状发作后4小时内被随机分配,分别接受茴酰化纤溶酶原链激酶激活剂复合物(APSAC)治疗,5分钟内静脉注射30万单位;或接受常规肝素治疗,静脉推注5000国际单位。初始治疗4小时后,两组均重新使用肝素,剂量为每天500国际单位/千克。共有112例患者接受了茴酰化纤溶酶原链激酶激活剂复合物治疗,119例患者在症状发作后的平均188±62分钟内接受了肝素治疗。通过单光子发射计算机断层扫描估计梗死面积,并以占全心肌体积的百分比表示。茴酰化纤溶酶原链激酶激活剂复合物治疗组梗死相关动脉的开通率为77%,肝素治疗组为36%(p<0.001)。通过造影血管造影测定的左心室射血分数,茴酰化纤溶酶原链激酶激活剂复合物治疗组显著高于肝素治疗组(绝对差值为6个百分点)。茴酰化纤溶酶原链激酶激活剂复合物治疗组的梗死面积显著减少了31%(前壁梗死亚组减少33%[p<0.05],下壁梗死亚组减少16%,无统计学意义)。左心室射血分数值与梗死面积之间存在密切的负相关(r = -0.73,p<0.01)。总之,急性心肌梗死患者早期输注茴酰化纤溶酶原链激酶激活剂复合物可产生较高的早期开通率,显著限制梗死面积,并显著保留左心室收缩功能,主要体现在前壁梗死患者中。

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